Maria Valeria Raimondi, Benedetta Maggio, Demetrio Raffa, Fabiana Plescia, Stella Cascioferro, Gabriella Cancemi, Domenico Schillaci, Maria Grazia Cusimano, Maria Vitale and Giuseppe Daidone

European Journal of Medicinal Chemistry, 2012, 58, 64
DOI: 10.1016/j.ejmech.2012.09.041

Spectroscopic analysis and charge transfer interaction studies of 4-benzyloxy-2-nitroaniline insecticide: A density functional theoretical approach

D. Arul Dhas, I. Hubert Joe, S.D.D. Roy and S. Balachandran

Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015, 135, 583
DOI: 10.1016/j.saa.2014.06.137

A practical nickel-catalyzed reductive alkylation of amidophenyl bromides

Xuge Liu, Zhilin Yang, Ya-Min Li, Fan Yang, Liang Feng, Nengzhong Wang, Debiao Ma, Kwen-Jen Chang and Yuehai Shen

Tetrahedron, 2014, 70, 9522
DOI: 10.1016/j.tet.2014.10.061

Facile Access to cis‐2,6‐Disubstituted Tetrahydropyrans by Palladium‐Catalyzed Decarboxylative Allylation: Total Syntheses of (±)‐Centrolobine and (+)‐Decytospolides A and B

Jing Zeng, Yu Jia Tan, Jimei Ma, Min Li Leow, Davin Tirtorahardjo and Xue‐Wei Liu

Chemistry A European J, 2014, 20, 405
DOI: 10.1002/chem.201303328

Mononitration of N-(4-Methoxyphenyl)acetamide in continuous-flow: Kinetics study and process optimization

Zhiqun Yu, Lishan Geng, Zhaoyang Mu, Jiadi Zhou, Bingbing Chen and Yuyu Yang

Chemical Engineering and Processing - Process Intensification, 2025, 208, 110136
DOI: 10.1016/j.cep.2024.110136

Regioselective and efficient bromination of anilides on water using HBr and Selectfluor

Deqiang Liang, Xiangguang Li, Chaowu Wang, Qishan Dong, Baoling Wang and Hai Wang

Tetrahedron Letters, 2016, 57, 5390
DOI: 10.1016/j.tetlet.2016.10.092

Application of Thionyl Chloride-Alcohol System in Organic Synthesis

晓丽孙

JOCR, 2016, 04, 23
DOI: 10.12677/JOCR.2016.42004

Pd-Catalyzed Arylation Reactions with Phenol Diazonium Salts: Application in the Synthesis of Diarylheptanoids

Bernd Schmidt, Frank Hölter, Alexandra Kelling and Uwe Schilde

J. Org. Chem., 2011, 76, 3357
DOI: 10.1021/jo2002787

Chemoenzymatic total synthesis of four stereoisomers of centrolobine

Bollipalli Nagarjuna, Barla Thirupathi, Chunduri Venkata Rao and Debendra K. Mohapatra

Tetrahedron Letters, 2015, 56, 4916
DOI: 10.1016/j.tetlet.2015.06.084

Iterative Arylation of Itaconimides with Diazonium Salts through Electrophilic Palladium Catalysis: Divergent β-H-Elimination Pathways in Repetitive Matsuda–Heck Reactions

Nastja Riemer, Michael Shipman, Pablo Wessig and Bernd Schmidt

J. Org. Chem., 2019, 84, 5732
DOI: 10.1021/acs.joc.9b00627

Acetamidoarenediazonium Salts: Opportunities for Multiple Arene Functionalization

Bernd Schmidt, Nelli Elizarov, Nastja Riemer and Frank Hölter

Eur J Org Chem, 2015, 2015, 5826
DOI: 10.1002/ejoc.201500795

A flexible enantioselective synthesis of (+)-centrolobine and 5-epi-diospongin-A using asymmetric transfer hydrogenation/tandem Grubbs cross-metathesis/oxy-Michael reaction as key steps

Gullapalli Kumaraswamy and Dasa Rambabu

Tetrahedron: Asymmetry, 2013, 24, 196
DOI: 10.1016/j.tetasy.2013.01.005

Evolution and Synthetic Applications of the Heck–Matsuda Reaction: The Return of Arenediazonium Salts to Prominence

Jason G. Taylor, Angélica Venturini Moro and Carlos Roque D. Correia

Eur J Org Chem, 2011, 2011, 1403
DOI: 10.1002/ejoc.201001620

Styrylsulfonates and ‐Sulfonamides through Pd‐Catalysed Matsuda–Heck Reactions of Vinylsulfonic Acid Derivatives and Arenediazonium Salts

Bernd Schmidt, Felix Wolf and Heiko Brunner

Eur J Org Chem, 2016, 2016, 2972
DOI: 10.1002/ejoc.201600469

A Formal Intermolecular Iodolactonization Reaction Based on a Radical‐Ionic Sequence

David F. León‐Rayo, Maricela Morales‐Chamorro and Alejandro Cordero‐Vargas

Eur J Org Chem, 2016, 2016, 1739
DOI: 10.1002/ejoc.201600051

Mizoroki–Heck Reactions with 4‐Phenoldiazonium Salts

Bernd Schmidt, Frank Hölter, René Berger and Sönke Jessel

Adv Synth Catal, 2010, 352, 2463
DOI: 10.1002/adsc.201000493

Synthesis of 8-Aryl-Substituted Coumarins Based on Ring-Closing Metathesis and Suzuki–Miyaura Coupling: Synthesis of a Furyl Coumarin Natural Product fromGalipea panamensis

Bernd Schmidt, Stefan Krehl, Alexandra Kelling and Uwe Schilde

J. Org. Chem., 2012, 77, 2360
DOI: 10.1021/jo2026564

Stereoselective Synthesis of Aza Analogues of Isoaltholactone and Goniothalesdiol – New Applications of the Heck–Matsuda Reaction

Angélica Venturini Moro, Marcelo Rodrigues dos Santos and Carlos Roque D. Correia

Eur J Org Chem, 2011, 2011, 7259
DOI: 10.1002/ejoc.201100886

Synthesis of (13C-Methoxy)Methacetin for Isotopic Breath Tests

A. R. El’man, I. E. Davydov, L. O. Kononov, A. I. Zinin and S. N. Dugin

Pharm Chem J, 2014, 48, 279
DOI: 10.1007/s11094-014-1094-7

Systematic Investigation into the Matsuda–Heck Reaction of α-Methylene Lactones: How Conformational Constraints Direct the β-H-Elimination Step

Bernd Schmidt, Felix Wolf and Christopher Ehlert

J. Org. Chem., 2016, 81, 11235
DOI: 10.1021/acs.joc.6b02207

Fear of the Dark: Diazo Printing by Photochemical Decomposition of Aryldiazonium Tetrafluoroborates

Fabio Parmeggiani

J. Chem. Educ., 2014, 91, 692
DOI: 10.1021/ed400555a

Ru‐ and Pd‐Catalysed Synthesis of 2‐Arylfurans by One‐Flask Heck Arylation/Oxidation

Bernd Schmidt and Diana Geißler

Eur J Org Chem, 2011, 2011, 4814
DOI: 10.1002/ejoc.201100549

Palladium Nanoparticles Supported on Sulfonic Acid Functionalized Silica as Trifunctional Heterogeneous Catalysts for Heck and Suzuki Reactions

Nicolas Oger, Erwan Le Grognec and François‐Xavier Felpin

ChemCatChem, 2015, 7, 2085
DOI: 10.1002/cctc.201500179

Synthesis of Arylidene-β-lactams via exo-Selective Matsuda-Heck Arylation of Methylene-β-lactams

Nastja Riemer, Martin Riemer, Mandy Krüger, Guy J. Clarkson, Michael Shipman and Bernd Schmidt

J. Org. Chem., 2021, 86, 8786
DOI: 10.1021/acs.joc.1c00638

Using Aryl Diazonium Salts in Palladium-Catalyzed Reactions under Safer Conditions

Nicolas Oger, Martin d’Halluin, Erwan Le Grognec and François-Xavier Felpin

Org. Process Res. Dev., 2014, 18, 1786
DOI: 10.1021/op500299t

Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives

Eslam Salahifar, Davood Nematollahi, Mehdi Bayat, Amir Mahyari and Hadi Amiri Rudbari

Org. Lett., 2015, 17, 4666
DOI: 10.1021/acs.orglett.5b01837

Matsuda–Heck Arylation of Glycals for the Stereoselective Synthesis of Aryl C-Glycosides

Fabian Otte and Bernd Schmidt

J. Org. Chem., 2019, 84, 14816
DOI: 10.1021/acs.joc.9b02410

Aryl Diazonium versus Iodonium Salts: Preparation, Applications and Mechanisms for the Suzuki–Miyaura Cross‐Coupling Reaction

Hélène Bonin, Eric Fouquet and François‐Xavier Felpin

Adv Synth Catal, 2011, 353, 3063
DOI: 10.1002/adsc.201100531

Regioselective ortho-nitration of N-phenyl carboxamides and primary anilines using bismuth nitrate/acetic anhydride

Yang Lu, Yaming Li, Rong Zhang, Kun Jin and Chunying Duan

Tetrahedron, 2013, 69, 9422
DOI: 10.1016/j.tet.2013.08.076

Dual Role of Acetanilides: Traceless Removal of a Directing Group through Deacetylation/Diazotation and Palladium-Catalyzed C–C-Coupling Reactions

Bernd Schmidt, Nelli Elizarov, Uwe Schilde and Alexandra Kelling

J. Org. Chem., 2015, 80, 4223
DOI: 10.1021/acs.joc.5b00272

Total Synthesis of Aqabamycin G, a Nitrophenyl Indolylmaleimide Marine Alkaloid from Vibrio sp. WMBA

Didier F. Vargas, Teodoro S. Kaufman and Enrique L. Larghi

J. Org. Chem., 2022, 87, 13494
DOI: 10.1021/acs.joc.2c00063

Combining Sanford Arylations on Benzodiazepines with the Nuisance Effect

Raysa Khan, Sarote Boonseng, Paul D. Kemmitt, Robert Felix, Simon J. Coles, Graham J. Tizzard, Gareth Williams, Olivia Simmonds, Jessica‐Lily Harvey, John Atack, Hazel Cox and John Spencer

Adv Synth Catal, 2017, 359, 3261
DOI: 10.1002/adsc.201700626

Unprecedented Substoichiometric Use of Hazardous Aryl Diazonium Salts in the Heck-Matsuda Reaction via a Double Catalytic Cycle

François Le Callonnec, Eric Fouquet and François-Xavier Felpin

Org. Lett., 2011, 13, 2646
DOI: 10.1021/ol200752x

Synthesis of (+)‐Centrolobine and Its Analogues by Using Acyl Anion Chemistry

Kasireddy Sudarshan and Indrapal Singh Aidhen

Eur J Org Chem, 2013, 2013, 2298
DOI: 10.1002/ejoc.201300097

Concise Stereoselective Total Synthesis of (−)-Hedycoropyran A

Byeongyeon Ahn, Ryangha Lee, Hyoungsu Kim and Dongjoo Lee

J. Org. Chem., 2023, 88, 17172
DOI: 10.1021/acs.joc.3c02046

Synthesis of indanones by sequential Heck-reduction–cyclization–alkylation (HRCA) reactions

Luma Nassar-Hardy, Sandy Fabre, Atef M. Amer, Eric Fouquet and François-Xavier Felpin

Tetrahedron Letters, 2012, 53, 338
DOI: 10.1016/j.tetlet.2011.11.042

A facile and efficient method for the selective deacylation of N-arylacetamides and 2-chloro-N-arylacetamides catalyzed by SOCl2

Gong-Bao Wang, Lin-Fa Wang, Chao-Zhang Li, Jing Sun, Guang-Ming Zhou and Da-Cheng Yang

Res Chem Intermed, 2012, 38, 77
DOI: 10.1007/s11164-011-0327-6

2,2′-Biphenols via Protecting Group-Free Thermal or Microwave-Accelerated Suzuki–Miyaura Coupling in Water

Bernd Schmidt, Martin Riemer and Manfred Karras

J. Org. Chem., 2013, 78, 8680
DOI: 10.1021/jo401398n